RU2589053C1 - ПИРРОЛО[2,1-f][1,2,4]ТРИАЗИНОВОЕ СОЕДИНЕНИЕ, СПОСОБ ЕГО ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ - Google Patents
ПИРРОЛО[2,1-f][1,2,4]ТРИАЗИНОВОЕ СОЕДИНЕНИЕ, СПОСОБ ЕГО ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ Download PDFInfo
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- RU2589053C1 RU2589053C1 RU2014147863/04A RU2014147863A RU2589053C1 RU 2589053 C1 RU2589053 C1 RU 2589053C1 RU 2014147863/04 A RU2014147863/04 A RU 2014147863/04A RU 2014147863 A RU2014147863 A RU 2014147863A RU 2589053 C1 RU2589053 C1 RU 2589053C1
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- Prior art keywords
- compound
- pyrrolo
- methyl
- mmol
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- 0 CC1(*)C=C(*)C(c(nc2*)n[n]3c2cc(C*)c3)=C*=C1 Chemical compound CC1(*)C=C(*)C(c(nc2*)n[n]3c2cc(C*)c3)=C*=C1 0.000 description 5
- CPVICAPKEDXVPO-UHFFFAOYSA-N CC(C)(C)C(Nc1ncc(C=O)c(C(F)(F)F)c1)=O Chemical compound CC(C)(C)C(Nc1ncc(C=O)c(C(F)(F)F)c1)=O CPVICAPKEDXVPO-UHFFFAOYSA-N 0.000 description 2
- QGLUXPFJGYXWQK-UHFFFAOYSA-N CC(C)(C)C(Nc(cc1C(F)(F)F)ncc1Br)=O Chemical compound CC(C)(C)C(Nc(cc1C(F)(F)F)ncc1Br)=O QGLUXPFJGYXWQK-UHFFFAOYSA-N 0.000 description 1
- LFUKOSKIHMCCDS-UHFFFAOYSA-N CC(OCc1cccc(-c(nc2N3CCOCC3)n[n]3c2cc(C)c3)c1)=O Chemical compound CC(OCc1cccc(-c(nc2N3CCOCC3)n[n]3c2cc(C)c3)c1)=O LFUKOSKIHMCCDS-UHFFFAOYSA-N 0.000 description 1
- KWXWZXVRCMYXHG-UHFFFAOYSA-N CC(OCc1cccc(C(NC2=O)=N[n]3c2cc(C(OC)=O)c3)c1)=O Chemical compound CC(OCc1cccc(C(NC2=O)=N[n]3c2cc(C(OC)=O)c3)c1)=O KWXWZXVRCMYXHG-UHFFFAOYSA-N 0.000 description 1
- VIYPPSOVHIRKCV-UHFFFAOYSA-N CCNC(Nc(nc1)cc(C(F)(F)F)c1-c(nc1N2CCOCC2)n[n]2c1cc(CN(CC1)CCN1S(C)(=O)=O)c2)=O Chemical compound CCNC(Nc(nc1)cc(C(F)(F)F)c1-c(nc1N2CCOCC2)n[n]2c1cc(CN(CC1)CCN1S(C)(=O)=O)c2)=O VIYPPSOVHIRKCV-UHFFFAOYSA-N 0.000 description 1
- VDDZOFLILWFGHD-UHFFFAOYSA-N CCOC(Nc(cc1C(F)(F)F)ncc1-c(nc1N2CCOCC2)n[n]2c1cc(CN(CC1)CCN1S(C)(=O)=O)c2)=O Chemical compound CCOC(Nc(cc1C(F)(F)F)ncc1-c(nc1N2CCOCC2)n[n]2c1cc(CN(CC1)CCN1S(C)(=O)=O)c2)=O VDDZOFLILWFGHD-UHFFFAOYSA-N 0.000 description 1
- CDBOEVACXRFJHZ-UHFFFAOYSA-N CN(C)Cc(cc12)c[n]1nc(-c(cc1)ccc1NC(Nc(c(Cl)c1)ccc1Cl)=O)nc2N1CCOCC1 Chemical compound CN(C)Cc(cc12)c[n]1nc(-c(cc1)ccc1NC(Nc(c(Cl)c1)ccc1Cl)=O)nc2N1CCOCC1 CDBOEVACXRFJHZ-UHFFFAOYSA-N 0.000 description 1
- JHRZVQCLXPKPNB-UHFFFAOYSA-N COC(c(cc12)c[n]1nc(-c(cc1)ccc1[N+]([O-])=O)nc2N1CCOCC1)=O Chemical compound COC(c(cc12)c[n]1nc(-c(cc1)ccc1[N+]([O-])=O)nc2N1CCOCC1)=O JHRZVQCLXPKPNB-UHFFFAOYSA-N 0.000 description 1
- AFUFOYSAHFAROX-HNNXBMFYSA-N C[C@@H](COCC1)N1c1nc(-c2c(C(F)(F)F)cc(N)nc2)n[n]2c1cc(CN(CC1)CCN1S(C)(=O)=O)c2 Chemical compound C[C@@H](COCC1)N1c1nc(-c2c(C(F)(F)F)cc(N)nc2)n[n]2c1cc(CN(CC1)CCN1S(C)(=O)=O)c2 AFUFOYSAHFAROX-HNNXBMFYSA-N 0.000 description 1
- RWGBXAQMUBGGKQ-UHFFFAOYSA-N Nc1nccc(C(F)(F)F)c1 Chemical compound Nc1nccc(C(F)(F)F)c1 RWGBXAQMUBGGKQ-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201210177980.3A CN103450204B (zh) | 2012-05-31 | 2012-05-31 | 吡咯[2,1-f][1,2,4]并三嗪类化合物,其制备方法及用途 |
CN201210177980.3 | 2012-05-31 | ||
PCT/CN2013/074559 WO2013177983A1 (zh) | 2012-05-31 | 2013-04-23 | 吡咯[2,1-f][1,2,4]并三嗪类化合物,其制备方法及用途 |
Publications (1)
Publication Number | Publication Date |
---|---|
RU2589053C1 true RU2589053C1 (ru) | 2016-07-10 |
Family
ID=49672377
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2014147863/04A RU2589053C1 (ru) | 2012-05-31 | 2013-04-23 | ПИРРОЛО[2,1-f][1,2,4]ТРИАЗИНОВОЕ СОЕДИНЕНИЕ, СПОСОБ ЕГО ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ |
Country Status (14)
Country | Link |
---|---|
US (1) | US9447101B2 (zh) |
EP (1) | EP2857403B1 (zh) |
JP (1) | JP6067107B2 (zh) |
KR (1) | KR101824299B1 (zh) |
CN (1) | CN103450204B (zh) |
AU (1) | AU2013270326B2 (zh) |
BR (1) | BR112014029708B1 (zh) |
CA (1) | CA2874062C (zh) |
ES (1) | ES2703934T3 (zh) |
HK (1) | HK1203499A1 (zh) |
MX (1) | MX359207B (zh) |
RU (1) | RU2589053C1 (zh) |
SG (1) | SG11201407752YA (zh) |
WO (1) | WO2013177983A1 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2771311C2 (ru) * | 2017-08-15 | 2022-04-29 | Сиэсписи Чжунци Фармасьютикал Текнолоджи (Шишцзяжуан) Ко., Лтд. | Ингибитор fgfr и его медицинское применение |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9724352B2 (en) * | 2012-05-31 | 2017-08-08 | Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences | Pyrrolo[2,1-F[1,2,4]triazine compounds, preparation methods and applications thereof |
EP2948454B1 (en) | 2013-01-24 | 2017-05-31 | Council of Scientific & Industrial Research An Indian registered body incorporated under the Registration of Societies Act (Act XXI of 1860) | Triazine compounds and a process for preparation thereof |
EP3209665B1 (en) | 2014-10-22 | 2019-08-14 | Bristol-Myers Squibb Company | Substituted pyrrolotriazine amine compounds as pi3k inhibitors |
US10214537B2 (en) | 2014-10-22 | 2019-02-26 | Bristol-Myers Squibb Company | Bicyclic heteroaryl amine compounds |
WO2017004134A1 (en) * | 2015-06-29 | 2017-01-05 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
WO2017040448A1 (en) * | 2015-08-31 | 2017-03-09 | Bristol-Myers Squibb Company | Tgf beta receptor antagonists |
CA3028822C (en) * | 2016-06-25 | 2021-06-22 | Suzhou Kintor Pharmaceuticals, Inc. | Mechanistic target of rapamycin signaling pathway inhibitors and therapeutic applications thereof |
CN109111447A (zh) * | 2017-06-23 | 2019-01-01 | 中国科学院上海药物研究所 | 7-位取代吡咯并三嗪类化合物或其药学上可用的盐,及其制备方法和用途 |
GB201720989D0 (en) * | 2017-12-15 | 2018-01-31 | Glaxosmithkline Ip Dev Ltd | Chemical compounds |
MX2022003217A (es) | 2019-09-19 | 2022-06-29 | Totus Medicines Inc | Conjugados terapeuticos. |
CN112851563A (zh) * | 2020-12-30 | 2021-05-28 | 安徽金鼎医药股份有限公司 | N-氨基-3-氮杂双环[3,3,0]辛烷盐酸盐的合成工艺 |
WO2023035614A1 (zh) * | 2021-09-10 | 2023-03-16 | 上海海和药物研究开发股份有限公司 | 包含PI3Kα抑制剂的药物组合 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010002954A1 (en) * | 2008-07-02 | 2010-01-07 | Wyeth | (2-aryl-7h-pyrrolo[2,3-d]pyrimidin-4-yl)morpholine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses |
WO2011089400A1 (en) * | 2010-01-22 | 2011-07-28 | Centro Nacional De Investigaciones Oncológicas (Cnio) | Inhibitors of pi3 kinase |
WO2011141713A1 (en) * | 2010-05-13 | 2011-11-17 | Centro Nacional De Investigaciones Oncologicas (Cnio) | New bicyclic compounds as pi3-k and mtor inhibitors |
RU2448109C2 (ru) * | 2006-08-08 | 2012-04-20 | Чугаи Сейяку Кабусики Кайся | Производное пиримидина в качестве ингибитора pi3k и его применение |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6867300B2 (en) | 2000-11-17 | 2005-03-15 | Bristol-Myers Squibb Company | Methods for the preparation of pyrrolotriazine compounds useful as kinase inhibitors |
TWI329112B (en) | 2002-07-19 | 2010-08-21 | Bristol Myers Squibb Co | Novel inhibitors of kinases |
TW200420565A (en) | 2002-12-13 | 2004-10-16 | Bristol Myers Squibb Co | C-6 modified indazolylpyrrolotriazines |
MY145634A (en) | 2003-12-29 | 2012-03-15 | Bristol Myers Squibb Co | Pyrrolotriazine compounds as kinase inhibitors |
WO2006044687A2 (en) * | 2004-10-15 | 2006-04-27 | Takeda San Diego, Inc. | Kinase inhibitors |
US7151176B2 (en) | 2004-10-21 | 2006-12-19 | Bristol-Myers Squibb Company | Pyrrolotriazine compounds |
TW200635927A (en) | 2004-12-22 | 2006-10-16 | Bristol Myers Squibb Co | Synthetic process |
US7619083B2 (en) | 2005-07-01 | 2009-11-17 | Bristol-Myers Squibb Company | Intermediates useful in preparing certain pyrrolotriazine compounds and process for making such intermediates |
US7514435B2 (en) | 2005-11-18 | 2009-04-07 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
JP5185930B2 (ja) | 2006-07-07 | 2013-04-17 | ブリストル−マイヤーズ スクイブ カンパニー | ピロロトリアジンキナーゼ阻害剤 |
KR101460816B1 (ko) * | 2006-12-07 | 2014-11-12 | 에프. 호프만-라 로슈 아게 | 포스포이노시타이드 3-키나제 억제제 화합물 및 그의 사용 방법 |
US8148522B2 (en) | 2007-01-02 | 2012-04-03 | Bristol-Myers Squibb Company | Intermediate useful in preparing certain pyrrolotriazine compounds and a process for making the intermediate |
EP2134716A1 (en) | 2007-04-18 | 2009-12-23 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
US8124759B2 (en) | 2007-05-09 | 2012-02-28 | Abbott Laboratories | Inhibitors of protein kinases |
EP2212333A1 (en) * | 2007-10-16 | 2010-08-04 | Wyeth LLC | Thienopyrimidine and pyrazolopyrimidine compounds and their use as mtor kinase and pi3 kinase inhibitors |
CL2009000241A1 (es) * | 2008-02-07 | 2010-09-03 | Chugai Pharmaceutical Co Ltd | Compuestos derivados de 5-(2-morfolin-4-il-7h-pirrolo[2,3-d]pirimidin-4-il)pirimidin-2-ilamina; proceso de preparacion; composicion farmaceutica; y uso de los compuestos para tratar o prevenir una enfermedad proliferativa tal como el cancer. |
WO2010002472A1 (en) | 2008-07-02 | 2010-01-07 | Ambit Biosciences Corporation | Jak kinase modulating compounds and methods of use thereof |
WO2010092340A1 (en) * | 2009-02-13 | 2010-08-19 | Ucb Pharma S.A. | Fused pyridine and pyrazine derivatives as kinase inhibitors |
EP2419429B1 (en) * | 2009-04-16 | 2014-03-26 | Centro Nacional de Investigaciones Oncológicas (CNIO) | Imidazopyrazines as inhibitors of protein kinases |
CN102675323B (zh) * | 2012-06-01 | 2014-04-09 | 南京药石药物研发有限公司 | 吡咯并[2,1-f][1,2,4]三嗪衍生物及其抗肿瘤用途 |
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2012
- 2012-05-31 CN CN201210177980.3A patent/CN103450204B/zh active Active
-
2013
- 2013-04-23 MX MX2014014622A patent/MX359207B/es active IP Right Grant
- 2013-04-23 BR BR112014029708-8A patent/BR112014029708B1/pt active IP Right Grant
- 2013-04-23 US US14/403,014 patent/US9447101B2/en active Active
- 2013-04-23 SG SG11201407752YA patent/SG11201407752YA/en unknown
- 2013-04-23 JP JP2015514329A patent/JP6067107B2/ja active Active
- 2013-04-23 ES ES13798006T patent/ES2703934T3/es active Active
- 2013-04-23 RU RU2014147863/04A patent/RU2589053C1/ru active
- 2013-04-23 CA CA2874062A patent/CA2874062C/en active Active
- 2013-04-23 WO PCT/CN2013/074559 patent/WO2013177983A1/zh active Application Filing
- 2013-04-23 AU AU2013270326A patent/AU2013270326B2/en active Active
- 2013-04-23 KR KR1020147033824A patent/KR101824299B1/ko active IP Right Grant
- 2013-04-23 EP EP13798006.6A patent/EP2857403B1/en active Active
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2015
- 2015-04-27 HK HK15104065.5A patent/HK1203499A1/zh unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2448109C2 (ru) * | 2006-08-08 | 2012-04-20 | Чугаи Сейяку Кабусики Кайся | Производное пиримидина в качестве ингибитора pi3k и его применение |
WO2010002954A1 (en) * | 2008-07-02 | 2010-01-07 | Wyeth | (2-aryl-7h-pyrrolo[2,3-d]pyrimidin-4-yl)morpholine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses |
WO2011089400A1 (en) * | 2010-01-22 | 2011-07-28 | Centro Nacional De Investigaciones Oncológicas (Cnio) | Inhibitors of pi3 kinase |
WO2011141713A1 (en) * | 2010-05-13 | 2011-11-17 | Centro Nacional De Investigaciones Oncologicas (Cnio) | New bicyclic compounds as pi3-k and mtor inhibitors |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2771311C2 (ru) * | 2017-08-15 | 2022-04-29 | Сиэсписи Чжунци Фармасьютикал Текнолоджи (Шишцзяжуан) Ко., Лтд. | Ингибитор fgfr и его медицинское применение |
Also Published As
Publication number | Publication date |
---|---|
BR112014029708A8 (pt) | 2021-09-08 |
HK1203499A1 (zh) | 2015-10-30 |
ES2703934T3 (es) | 2019-03-13 |
WO2013177983A1 (zh) | 2013-12-05 |
CN103450204B (zh) | 2016-08-17 |
BR112014029708B1 (pt) | 2023-05-02 |
EP2857403A1 (en) | 2015-04-08 |
AU2013270326B2 (en) | 2016-07-14 |
CA2874062A1 (en) | 2013-12-05 |
US9447101B2 (en) | 2016-09-20 |
KR20150009565A (ko) | 2015-01-26 |
SG11201407752YA (en) | 2015-01-29 |
JP6067107B2 (ja) | 2017-01-25 |
JP2015518010A (ja) | 2015-06-25 |
EP2857403A4 (en) | 2015-10-21 |
KR101824299B1 (ko) | 2018-03-14 |
US20150141644A1 (en) | 2015-05-21 |
MX2014014622A (es) | 2015-08-10 |
CA2874062C (en) | 2015-09-22 |
EP2857403B1 (en) | 2018-10-10 |
CN103450204A (zh) | 2013-12-18 |
BR112014029708A2 (pt) | 2017-06-27 |
AU2013270326A1 (en) | 2014-12-18 |
MX359207B (es) | 2018-09-19 |
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